Phosphoenolpyruvate

Details

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Internal ID 0fcd7fff-8461-46a6-bacc-1d176b7865da
Taxonomy Organic acids and derivatives > Organic phosphoric acids and derivatives > Phosphate esters
IUPAC Name 2-phosphonooxyprop-2-enoic acid
SMILES (Canonical) C=C(C(=O)O)OP(=O)(O)O
SMILES (Isomeric) C=C(C(=O)O)OP(=O)(O)O
InChI InChI=1S/C3H5O6P/c1-2(3(4)5)9-10(6,7)8/h1H2,(H,4,5)(H2,6,7,8)
InChI Key DTBNBXWJWCWCIK-UHFFFAOYSA-N
Popularity 13,621 references in papers

Physical and Chemical Properties

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Molecular Formula C3H5O6P
Molecular Weight 168.04 g/mol
Exact Mass 167.98237487 g/mol
Topological Polar Surface Area (TPSA) 104.00 Ų
XlogP -1.10
Atomic LogP (AlogP) -0.31
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 3

Synonyms

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Phosphoenolpyruvic acid
138-08-9
2-(phosphonooxy)prop-2-enoic acid
2-Phosphonooxyprop-2-enoic acid
2-(phosphonooxy)-2-propenoic acid
545YL308OW
2-(phosphonooxy)-2-propenoate
CHEBI:44897
DTXSID80861797
CHEBI:18021
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Phosphoenolpyruvate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.6944 69.44%
Caco-2 - 0.7996 79.96%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability - 0.7429 74.29%
Subcellular localzation Mitochondria 0.8081 80.81%
OATP2B1 inhibitior - 0.8622 86.22%
OATP1B1 inhibitior + 0.9698 96.98%
OATP1B3 inhibitior + 0.9448 94.48%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9713 97.13%
P-glycoprotein inhibitior - 0.9666 96.66%
P-glycoprotein substrate - 0.9914 99.14%
CYP3A4 substrate - 0.6794 67.94%
CYP2C9 substrate + 0.5973 59.73%
CYP2D6 substrate - 0.8886 88.86%
CYP3A4 inhibition - 0.9346 93.46%
CYP2C9 inhibition - 0.8642 86.42%
CYP2C19 inhibition - 0.8336 83.36%
CYP2D6 inhibition - 0.9013 90.13%
CYP1A2 inhibition - 0.8775 87.75%
CYP2C8 inhibition - 0.9700 97.00%
CYP inhibitory promiscuity - 0.9688 96.88%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5846 58.46%
Carcinogenicity (trinary) Non-required 0.5971 59.71%
Eye corrosion + 0.6036 60.36%
Eye irritation - 0.5993 59.93%
Skin irritation - 0.5893 58.93%
Skin corrosion - 0.5395 53.95%
Ames mutagenesis - 0.7100 71.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8405 84.05%
Micronuclear + 0.5800 58.00%
Hepatotoxicity + 0.5750 57.50%
skin sensitisation - 0.5533 55.33%
Respiratory toxicity + 0.6222 62.22%
Reproductive toxicity - 0.7222 72.22%
Mitochondrial toxicity + 0.7750 77.50%
Nephrotoxicity + 0.7783 77.83%
Acute Oral Toxicity (c) III 0.5574 55.74%
Estrogen receptor binding - 0.8090 80.90%
Androgen receptor binding - 0.8660 86.60%
Thyroid receptor binding - 0.7757 77.57%
Glucocorticoid receptor binding - 0.8923 89.23%
Aromatase binding - 0.6799 67.99%
PPAR gamma - 0.5000 50.00%
Honey bee toxicity - 0.7108 71.08%
Biodegradation + 0.6500 65.00%
Crustacea aquatic toxicity - 0.6855 68.55%
Fish aquatic toxicity + 0.9492 94.92%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL340 P08684 Cytochrome P450 3A4 82.63% 91.19%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 80.42% 87.67%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 80.31% 96.09%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
There are no matching plants.

Cross-Links

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PubChem 1005
NPASS NPC116125
ChEMBL CHEMBL1235228
LOTUS LTS0250994
wikiData Q412139